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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095017copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-3,294,608 , GRCh38.p12 chr16: 3,243,141-3,244,608 MEFV
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 more genes
    nsv7094668copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,306,291-3,306,587 , GRCh38.p12 chr16: 3,256,291-3,256,587 MEFV
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv6977592copy number variation1nstd229human GRCh38 chr16: 3,246,328-3,262,674 , GRCh37.p13 chr16: 3,296,328-3,312,674 LINC00921, MEFV
    nsv6974280copy number variation1nstd229human GRCh38 chr16: 3,125,283-3,274,634 , GRCh37.p13 chr16: 3,175,284-3,324,634 TRK-CTT4-1, ZNF200, 23 more genes
    nsv6971314copy number variation1nstd229human GRCh38 chr16: 3,243,699-3,253,429 , GRCh37.p13 chr16: 3,293,699-3,303,429 MEFV
    nsv6968778copy number variation1nstd229human GRCh38 chr16: 3,206,227-3,444,939 , GRCh37.p13 chr16: 3,256,227-3,494,939 MEFV, ZNF597, 18 more genes
    nsv6968061copy number variation1nstd229human GRCh38 chr16: 3,174,701-3,284,700 , GRCh37.p13 chr16: 3,224,702-3,334,700 MEFV, TRP-TGG3-5, 14 more genes
    nsv6967022copy number variation1nstd229human GRCh38 chr16: 3,162,501-3,250,100 , GRCh37.p13 chr16: 3,212,502-3,300,100 TRK-CTT4-1, ZNF200, 14 more genes
    nsv6966465copy number variation1nstd229human GRCh38 chr16: 3,206,167-3,270,350 , GRCh37.p13 chr16: 3,256,167-3,320,350 OR1F2P, MEFV, 3 more genes
    nsv6963020copy number variation1nstd229human GRCh38 chr16: 3,240,258-3,240,397 , GRCh37.p13 chr16: 3,290,258-3,290,397 MEFV
    nsv6961195copy number variation1nstd229human GRCh38 chr16: 3,242,518-3,245,135 , GRCh37.p13 chr16: 3,292,518-3,295,135 MEFV
    nsv6960235copy number variation1nstd229human GRCh38 chr16: 3,242,343-3,255,300 , GRCh37.p13 chr16: 3,292,343-3,305,300 MEFV
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6509422copy number variation1nstd223human GRCh38 chr16: 3,161,768-3,335,002 , GRCh37.p13 chr16: 3,211,769-3,385,002 TRP-TGG4-1, LINC00921, 19 more genes
    nsv6310075copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,304,138-3,306,587 , GRCh38.p12 chr16: 3,254,138-3,256,587 MEFV
    nsv6310074copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,293,141-3,929,917 , GRCh38.p12 chr16: 3,243,141-3,879,916 MTRNR2L4, TRAP1, 26 more genes
    nsv6310073copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-3,297,266 , GRCh38.p12 chr16: 3,243,141-3,247,266 MEFV
    nsv6290044copy number variation1nstd218human GRCh38.p12 chr16: 2,757,479-3,781,321 , GRCh37 chr16: 2,807,480-3,831,322 , CREBBP, 87 more genes
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